The polymorphic expression of cytochrome P-450 genes appears to be an important factor in adverse reactions to drugs, environmental toxins and chemical carcinogens. An understanding of the molecular basis of these polymorphisms may enable prediction and prevention of some of these effects. The high degree of polymorphism of this multigene family and scattered distribution of the subfamilies in the human genome may well provide useful markers for gene mapping and the study of genetic linkage in human disease.</p
The cytochrome P450 (CYP) enzymes are major players in drug metabolism. More than 2,000 mutations ha...
Inherited genetic traits co-determine the susceptibility of an individual to a toxic chemical. Speci...
THE mammalian cytochrome P450-dependent monooxygenase system is involved in the metabolism of drugs ...
The polymorphic expression of cytochrome P-450 genes appears to be an important factor in adverse re...
Cytochromes P-450 are a superfamily of hemoproteins which represent the main pathway for drug and ch...
The cytochrome P450 isoenzymes are a super family of haemoproteins that are terminal oxidases of mix...
Inhibitors of some cytochrome P450s (CYPs) are used to design target-specific drugs. CYPs belonging ...
The vast majority of cancers arise as a consequence of exposure to environmental agents that are tox...
Hepatic oxidation is a major drug metabolising process and is carried out by the cytochrome P-450 mo...
Pharmacogenetics is the study of how interindividual variations in the DNA sequence of specific gene...
Since the majority of chemical carcinogens are not capable of causing hazardous effects per se, the ...
Cytochrome P450 is an enzyme involved in the metabolism of phase 1 xenobiotics, toxins, endogenous h...
There are 18 mammalian cytochrome P450 (CYP) families, which encode 57 genes in the human genome. CY...
A protocol to work on the «Cybertory» virtual laboratory at Biomodel.UAH.es Genetic diversity of ind...
The cytochrome P450 (CYP) enzymes are major players in drug metabolism. More than 2,000 mutations ha...
The cytochrome P450 (CYP) enzymes are major players in drug metabolism. More than 2,000 mutations ha...
Inherited genetic traits co-determine the susceptibility of an individual to a toxic chemical. Speci...
THE mammalian cytochrome P450-dependent monooxygenase system is involved in the metabolism of drugs ...
The polymorphic expression of cytochrome P-450 genes appears to be an important factor in adverse re...
Cytochromes P-450 are a superfamily of hemoproteins which represent the main pathway for drug and ch...
The cytochrome P450 isoenzymes are a super family of haemoproteins that are terminal oxidases of mix...
Inhibitors of some cytochrome P450s (CYPs) are used to design target-specific drugs. CYPs belonging ...
The vast majority of cancers arise as a consequence of exposure to environmental agents that are tox...
Hepatic oxidation is a major drug metabolising process and is carried out by the cytochrome P-450 mo...
Pharmacogenetics is the study of how interindividual variations in the DNA sequence of specific gene...
Since the majority of chemical carcinogens are not capable of causing hazardous effects per se, the ...
Cytochrome P450 is an enzyme involved in the metabolism of phase 1 xenobiotics, toxins, endogenous h...
There are 18 mammalian cytochrome P450 (CYP) families, which encode 57 genes in the human genome. CY...
A protocol to work on the «Cybertory» virtual laboratory at Biomodel.UAH.es Genetic diversity of ind...
The cytochrome P450 (CYP) enzymes are major players in drug metabolism. More than 2,000 mutations ha...
The cytochrome P450 (CYP) enzymes are major players in drug metabolism. More than 2,000 mutations ha...
Inherited genetic traits co-determine the susceptibility of an individual to a toxic chemical. Speci...
THE mammalian cytochrome P450-dependent monooxygenase system is involved in the metabolism of drugs ...